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Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout
Isothermal, cell-free, synthetic biology-based approaches to pathogen detection leverage the power of tools available in biological systems, such as highly active polymerases compatible with lyophilization, without the complexity inherent to live-cell systems, of which nucleic acid sequence based am...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430665/ https://www.ncbi.nlm.nih.gov/pubmed/32482894 http://dx.doi.org/10.1261/rna.075192.120 |
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author | Aufdembrink, Lauren M. Khan, Pavana Gaut, Nathaniel J. Adamala, Katarzyna P. Engelhart, Aaron E. |
author_facet | Aufdembrink, Lauren M. Khan, Pavana Gaut, Nathaniel J. Adamala, Katarzyna P. Engelhart, Aaron E. |
author_sort | Aufdembrink, Lauren M. |
collection | PubMed |
description | Isothermal, cell-free, synthetic biology-based approaches to pathogen detection leverage the power of tools available in biological systems, such as highly active polymerases compatible with lyophilization, without the complexity inherent to live-cell systems, of which nucleic acid sequence based amplification (NASBA) is well known. Despite the reduced complexity associated with cell-free systems, side reactions are a common characteristic of these systems. As a result, these systems often exhibit false positives from reactions lacking an amplicon. Here we show that the inclusion of a DNA duplex lacking a promoter and unassociated with the amplicon fully suppresses false positives, enabling a suite of fluorescent aptamers to be used as NASBA tags (Apta-NASBA). Apta-NASBA has a 1 pM detection limit and can provide multiplexed, multicolor fluorescent readout. Furthermore, Apta-NASBA can be performed using a variety of equipment, for example, a fluorescence microplate reader, a qPCR instrument, or an ultra-low-cost Raspberry Pi-based 3D-printed detection platform using a cell phone camera module, compatible with field detection. |
format | Online Article Text |
id | pubmed-7430665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74306652021-09-01 Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout Aufdembrink, Lauren M. Khan, Pavana Gaut, Nathaniel J. Adamala, Katarzyna P. Engelhart, Aaron E. RNA Article Isothermal, cell-free, synthetic biology-based approaches to pathogen detection leverage the power of tools available in biological systems, such as highly active polymerases compatible with lyophilization, without the complexity inherent to live-cell systems, of which nucleic acid sequence based amplification (NASBA) is well known. Despite the reduced complexity associated with cell-free systems, side reactions are a common characteristic of these systems. As a result, these systems often exhibit false positives from reactions lacking an amplicon. Here we show that the inclusion of a DNA duplex lacking a promoter and unassociated with the amplicon fully suppresses false positives, enabling a suite of fluorescent aptamers to be used as NASBA tags (Apta-NASBA). Apta-NASBA has a 1 pM detection limit and can provide multiplexed, multicolor fluorescent readout. Furthermore, Apta-NASBA can be performed using a variety of equipment, for example, a fluorescence microplate reader, a qPCR instrument, or an ultra-low-cost Raspberry Pi-based 3D-printed detection platform using a cell phone camera module, compatible with field detection. Cold Spring Harbor Laboratory Press 2020-09 /pmc/articles/PMC7430665/ /pubmed/32482894 http://dx.doi.org/10.1261/rna.075192.120 Text en © 2020 Aufdembrink et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Article Aufdembrink, Lauren M. Khan, Pavana Gaut, Nathaniel J. Adamala, Katarzyna P. Engelhart, Aaron E. Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout |
title | Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout |
title_full | Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout |
title_fullStr | Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout |
title_full_unstemmed | Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout |
title_short | Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout |
title_sort | highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430665/ https://www.ncbi.nlm.nih.gov/pubmed/32482894 http://dx.doi.org/10.1261/rna.075192.120 |
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